Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2391769 | 0.925 | 0.040 | 1 | 96513405 | regulatory region variant | A/G;T | snv | 3 | |||
rs11210887 | 0.925 | 0.040 | 1 | 43610348 | intron variant | G/A | snv | 0.52 | 2 | ||
rs113551349 | 0.925 | 0.040 | 1 | 44009451 | intron variant | C/T | snv | 0.20 | 2 | ||
rs139868495 | 0.925 | 0.040 | 8 | 34805452 | intron variant | C/T | snv | 3.1E-02 | 2 | ||
rs145108385 | 0.925 | 0.040 | 5 | 43054645 | intron variant | A/G | snv | 2 | |||
rs1476535 | 0.925 | 0.040 | 7 | 114430980 | intron variant | C/G;T | snv | 2 | |||
rs2189012 | 0.925 | 0.040 | 7 | 114571857 | intron variant | G/A | snv | 0.73 | 2 | ||
rs2782639 | 0.925 | 0.040 | 1 | 43540668 | intron variant | A/G | snv | 0.26 | 2 | ||
rs4259397 | 0.925 | 0.040 | 8 | 92354062 | upstream gene variant | G/A;T | snv | 2 | |||
rs4858253 | 0.925 | 0.040 | 3 | 20687599 | intron variant | C/T | snv | 0.33 | 2 | ||
rs4916723 | 0.925 | 0.040 | 5 | 88558577 | intron variant | A/C;G;T | snv | 2 | |||
rs56319043 | 0.925 | 0.040 | 1 | 43705540 | intron variant | C/T | snv | 0.17 | 2 | ||
rs74760947 | 0.925 | 0.040 | 8 | 34495092 | intergenic variant | A/G | snv | 3.1E-02 | 2 | ||
rs76545266 | 0.925 | 0.040 | 8 | 34224003 | upstream gene variant | T/C | snv | 2.9E-02 | 2 | ||
rs797267 | 0.925 | 0.040 | 12 | 89373460 | intron variant | A/G | snv | 0.28 | 2 | ||
rs8039398 | 0.925 | 0.040 | 15 | 47438673 | intron variant | T/C | snv | 0.47 | 2 |